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Clinical Trial Manager - FSP ( Turkey)

82% Flex
Full Remote
Mid-level (2-5 years)
  • Remote from:Turkey
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Clinical Trial Manager - FSP ( Turkey)

82% Flex
Remote: Full Remote
Experience: Mid-level (2-5 years)
Work from: Turkey...

Offer summary

Qualifications:

At least 2 years leading clinical trials, Minimum of 5 years as a CRA, Solid background in project or people management.

Key responsabilities:

  • Supporting, coordinating and conducting regional and global clinical trials for clients
  • Involvement in study start-up, maintenance, closure, vendor management and CRA oversight
Parexel logo
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Parexel

Large

http://www.parexel.com/

10001 Employees

Job description

Logo Jobgether

Your missions

When our values align, there's no limit to what we can achieve.
 
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Clinical Trial Manager based in Istanbul or Ankara. Homebased.

Inviting applications to join our EMEA Clinical Operations Talent Pipeline. Please provide some basic information and upload your resume. As soon as the role becomes available, we will promptly send you an email invitation to officially

apply. Thank you for your interest.

At Parexel FSP people make a difference. We have a crucial mission: to prevent and cure disease by delivering important new medicines and therapies to patients in need. We achieve this important goal through the knowledge, expertise, innovation, and commitment of our employees around the world.

Dedicated to one sponsor, a global pharmaceutical company that leads the way in discovering and developing innovative health solutions that help prevent and treat diseases in animals and people.

Our sponsor has a long history of excellence in research, delivering medicines, vaccines, and other health solutions for some of the most difficult diseases in the world.

You will play a key role in supporting, coordinating, and conducting regional and global clinical trials for our clients. This includes full involvement in study start-up, maintenance, and closure, as well as vendor management and CRA oversight.

Expect exciting career challenges and exceptional financial rewards, training, and development. but with a healthy work-life balance. We value your well-being as much as that of our patients.

Experience required:

If you are a professional with 2 at least years of experience in leading clinical trials and a minimum of 5 years as a CRA, as well as a solid background in project

management or people management, we can offer you a stellar future.

Apply today!

#LI-TA1

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Required profile

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Experience

Level of experience :
Mid-level (2-5 years)
Spoken language(s)
Check out the description to know which languages are mandatory.

Soft Skills

  • Team player
  • Proactive mindset

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